VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
CGMP Deviations
What was recalled
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
- Recalling firm
- Profarma Distributors LLC
- Origin
- OH, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1041-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
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